Nonoyama M, Kawai Y, Pagano J S
Bibl Haematol. 1975(40):577-83. doi: 10.1159/000397575.
The presence of Epstein-Barr virus (EBV) DNA in biopsies of human tumors was tested by complementary RNA (cRNA) hybridization on membranes and DNA-DNA reassociation kinetics. DNA-DNA reassociation kinetics can detect as few as 1 EBV genome in every 50 cells, and the cRNA method can detect EBV genomes if 2 or more are present in a cell. Twenty-three out of 24 African Burkitt's lymphoma biopsies, 18 out of 23 African nasopharyngeal carcinomas (NPC), and 8 out of 24 other African tumors were positive for EBV DNA. Three cases of American Burkitt's lymphoma were tested by the cRNA method, and EBV DNA was not detected. Three out of 25 American tumors other than American Burkitt's lymphoma contained 0.1 to 0.3 genomes per cell of EBV DNA.
通过膜上的互补RNA(cRNA)杂交和DNA-DNA重缔合动力学检测人类肿瘤活检组织中爱泼斯坦-巴尔病毒(EBV)DNA的存在情况。DNA-DNA重缔合动力学能够检测出每50个细胞中低至1个EBV基因组,而cRNA方法在一个细胞中存在2个或更多EBV基因组时就能检测到。24例非洲伯基特淋巴瘤活检组织中有23例、23例非洲鼻咽癌(NPC)中有18例以及24例其他非洲肿瘤中有8例的EBV DNA呈阳性。采用cRNA方法检测了3例美国伯基特淋巴瘤,未检测到EBV DNA。除美国伯基特淋巴瘤外的25例美国肿瘤中有3例每细胞含有0.1至0.3个EBV DNA基因组。